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. 2019 Nov 27;17:156–173. doi: 10.1016/j.omtm.2019.11.016

Table 1.

Patient Samples

Cell Lines Clinical Diagnosis Mutation in A1 Mutation in A2 Reference
USH2A-USH-iPSC USH2 c.2299delG c.2299delG 29
USH2A-RP-iPSC non-syndromic arRP c.2276G>T c.2299delG 28,30

A1, allele 1; A2, allele 2.